Telehealth & Rehabilitation Advancing Chronic Condition Research Center

Partnering with patients to shape the future of digital health
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Explore the Telehealth & Rehabilitation Advancing Chronic Condition Research Center

Research

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People

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Publications

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Education

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Susan L Murphy
Principal Investigator

Susan Murphy, ScD, OTR, FAOTA

Dr. Murphy is an occupational therapist by training and Professor in the Department of Physical Medicine and Rehabilitation, and of Internal Medicine, Rheumatology Division at the University of Michigan. She also is a faculty lead in the Education and Mentoring Group at the Michigan Institute of Clinical and Health Research (MICHR). Her research interests involve developing and translating relevant and effective interventions into practice to optimize management of chronic conditions. She has a particular interest in advancing telehealth and rehabilitation for people with scleroderma and leads the behavioral studies branch of the University of Michigan's Scleroderma Program.

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Our Team in the Spotlight!


Spotlight on RENEW: Exploring Fatigue and Resilience in Spondyloarthritis Research

In the latest episode of Spondycast, University of Michigan researcher Susan Murphy, ScD, OTR, discusses the newly launched RENEW Study, a research initiative funded by the Spondylitis Association of America that focuses on understanding fatigue, energy management, and resilience in people living with spondyloarthritis. This conversation highlights the importance of addressing persistent fatigue—a common and often overlooked symptom in spondyloarthritis that can significantly impact quality of life—and explores innovative approaches to support patients’ energy and resilience. Tune in to gain insight into this emerging study and its potential to inform better strategies for managing fatigue in chronic inflammatory disease.

Listen to the podcast:

RENEW Your Energy: Inside a New Research Study on Fatigue and Resilience in Spondyloarthritis


Patients as Partners in Scleroderma Research

A recent feature in Michigan Medicine Health Lab highlights the innovative, patient-centered approach guiding scleroderma research at the TRACC-R Center. Individuals living with scleroderma are not only participating in studies — they are helping design them.

From shaping energy management interventions to refining study materials and ensuring research reflects real-life challenges, patient partners play a critical role in advancing meaningful, impactful work. Their lived experience strengthens our science and ensures that the programs we develop truly meet the needs of the community.

Read the full story: 

For scleroderma research, patients seen as essential co-creators


The American College of Rheumatology (ACR) Highlights Dr. Susan Murphy's Work in Participatory Research

We're thrilled to share that the ACR recently published a feature article spotlighting Dr. Susan Murphy's work in participatory research — empowering patients to co-design studies that truly reflect their lived experiences. 

Read the full story: 

Read the full story on ACR’s website


Patient Partner Sheri Hicks Speaks at the ACR Conference

Our amazing patient partner Sheri Hicks took the stage at the ACR’s Patient Perspectives session, sharing her journey in "Breaking Through Scleroderma’s Invisible Struggles: From Isolation to Connection." 

Watch Sheri Hick's talk about her journey with scleroderma: 


A Podcast Discussing Dr. Yen Chen's Brain Boost Program and Research on Cognitive Dysfunction in Scleroderma

Dr. Yen Chen talks about the definition of “brain fog,” its general causes, and how it affects people living with scleroderma. The discussion also covers activities and lifestyle strategies that can help improve memory, focus, and attention. Lots of great information and practical tips for managing brain fog. 

Listen to the podcast:

Mogil's Mobcast: A Scleroderma Chat


A Podcast Discussing Dr. Susan Murphy's Research and Advocacy in the Scleroderma Program

Ann Mogilevsky, a podcast creator and host of Mogil's Mobcast, talks with Dr. Susan Murphy and Mary Alore, our Peer Mentor and RENEW Health Coach. The discussion includes different programs being implemented at the university, such as the Scleroderma Peer Mentor Program, the Scleroderma Backers, and some of the research the university is doing. 

Listen to the podcast:

 Mogil's Mobcast: A Scleroderma Chat

Resources

Using this website, discover helpful tools that can help people with scleroderma navigate the scleroderma journey with confidence. This toolkit website was co-designed with scleroderma patients and rheumatologists.

Learn More: Scleroderma Toolkit Website

The RENEW app (Resilience-based Energy Management to Enhance Well-being app) allows individuals with scleroderma to set goals, track health behaviors, and receive feedback about goal progress to manage the symptoms of their condition.

Apple App Store | Google Play Store

The RENEW website (Resilience-based Energy Management to Enhance Well-being website ) contains all of the information from the RENEW app and has downloadable resource documents to set goals, and track progress.

Learn More: RENEW Website

The Scleroderma Program at Michigan Medicine, directed by Dinesh Khanna, MD, MSc and John Varga, MD, together with a group of experts, examines the causes and mechanisms of scleroderma in order to develop better, targeted treatment options and to improve the quality of life for people with scleroderma. 

Learn More: Michigan Medicine Scleroderma Program

A group of scleroderma patients from Michigan Medicine offering community support for other scleroderma patients all over the world! 

Learn More: Facebook Support Group page

A patient-led scleroderma and chronic illness community

The Chronic Crusaders are a passionate, patient-led community dedicated to empowering individuals living with scleroderma and other chronic illnesses—as well as their care partners. Through social gatherings, fundraising events, and informal education, the group fosters connection, awareness, and hope.

Their mission is to create a welcoming space where patients can find strength in shared experiences, gain practical knowledge, and inspire one another to live fully. By championing advocacy and education, the Chronic Crusaders help amplify patient voices and support research that drives meaningful change. 

Learn More: Chronic Crusaders

Contact Us

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24 Frank Lloyd Wright Drive,
Lobby M, Ste 3100
Ann Arbor, MI 48106-5737